首页工具

登录

搜索结果

Search Results for " anxiety-like "

14

抑制剂 & 化合物

1

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T16421	p-MPPI hydrochloride	5-HT Receptor	GPCR/G Protein; Neuroscience
	p-MPPI hydrochloride 是一种选择性的，具有高亲和力的5-HT1A 受体拮抗剂，能穿过血脑屏障，具有抗抑郁和抗焦虑样作用。
T7644	DPN Diarylpropionitrile,2,3-双(4-羟苯基)丙腈	Apoptosis; Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Autophagy	Apoptosis; Autophagy; Endocrinology/Hormones
	DPN (Diarylpropionitrile) 是一种非甾体雌激素受体 ERβ选择性配体，其 EC50值为 0.85 nM。DPN 在许多神经系统疾病具有神经保护作用。
T23444	TCS 1105 N-(4-fluorobenzyl)-2-(1H-indol-3-yl)-2-oxoacetamide	Others	Others
	TCS 1105是一种GABAA 苯并二氮卓受体（BZR）配体。TCS 1105阻断Sema3A 诱导的轴突生长锥塌陷。TCS 1105能减少小鼠的焦虑样行为，增强攻击性行为和社会支配力。
T5828	MS21570 5-(苄基硫代)-N-甲基-1,3,4-噻二唑-2-胺	GPR	Endocrinology/Hormones; GPCR/G Protein
	MS21570 作为 GPR171 拮抗剂基于其阻断能力，IC50 为 220 nM，可减少小鼠的焦虑样行为和恐惧条件反射。
T35707	3'-Sialyllactose sodium 3'-SL sodium	NF-κB	NF-κB
	3'-Sialyllactose sodium 是一种益生元，具有抗炎活性，可维持免疫稳态。3'-Sialyllactose sodium 可减少压力源引起的焦虑样行为，可用于研究炎症和关节炎。
T16401	Org-12962	5-HT Receptor	GPCR/G Protein; Neuroscience
	Org-12962 是选择性，具有口服活性的 5-HT2C 受体激动剂，pEC50 值为 7.01。 Org-12962 对 5-HT2A 和 5-HT2B 受体也具有很高的作用，pEC50 分别为 6.38 和 6.28。Org-12962 在焦虑大鼠的模型中显示出缓解作用。
TP1982	Neuropeptide S(Rat) Neuropeptide S (Rat)
	Potent endogenous neuropeptide S receptor (NSPR) agonist (EC50 = 3.2 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
T75951	Neuropeptide S(Rat) TFA
	Neuropeptide S(Rat) TFA, a robust endogenous agonist for the neuropeptide S receptor (NSPR) with an EC50 of 3.2 nM, enhances locomotor activity and promotes wakefulness while concurrently diminishing anxiety-like behavior in mice.
TP1983	Neuropeptide S (human)
	Potent endogenous neuropeptide S receptor agonist (EC50 = 9.4 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
TP1981	Neuropeptide S(Mouse) Neuropeptide S (Mouse)
	Potent endogenous neuropeptide S receptor (NPSR) agonist (EC50 = 3 nM). Induces mobilization of intracellular Ca2+. Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
T75950	Neuropeptide S(Mouse) TFA
	Neuropeptide S(Mouse) TFA, an endogenous agonist for the neuropeptide S receptor (NPSR) with an EC50 value of 3 nM, plays a significant role in physiological processes by inducing the mobilization of intracellular Ca2+. This compound elevates locomotor activity and wakefulness, and simultaneously decreases anxiety-like behavior in mice.
T83665	α-Helical CRF (9-41) TFA α-Helical Corticotropin-Releasing Factor (9-41)
	α-Helical CRF (9-41) 是一种合成的皮质酮释放因子（CRF）拮抗剂。它在0.5至5 µM浓度范围内，能抑制CRF诱导的大鼠前叶垂体细胞释放促肾上腺皮质激素（ACTH）。在体内研究中，α-Helical CRF (9-41) (0.02-0.6 µmol/kg) 能够抑制未经麻醉的完整大鼠体内CRF诱导的ACTH释放，并在0.6 µmol/kg剂量下抑制大鼠应激诱导的ACTH释放。此外，α-Helical CRF (9-41) 在尼古丁诱导的条件性焦虑大鼠模型中增加社交互动时间，并减少小鼠的类似暴饮暴食的乙醇消费。
T37114	SB 242084 dihydrochloride
	SB 242084 hydrochloride is a 5-HT2C receptor antagonist(pKi=9.0) that displays 158- and 100-fold selectivity over 5-HT2A and 5-HT2B receptors respectively.IC50 value: 9.0(pKi) [1]Target: 5-HT2C antagonistin vitro: SB 242084 had over 100-fold selectivity over a range of other 5-HT, dopamine and adrenergic receptors. In studies of 5-HT-stimulated phosphatidylinositol hydrolysis using SH-SY5Y cells stably expressing the cloned human 5-HT2C receptor, SB 242084 acted as an antagonist with a pKb of 9....
T38145	Eltoprazine
	Eltoprazine(DU28853) is a serenic or antiaggressive agent which as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor.IC50 value:Target: 5-HT1A/1B agonist; 5-HT2C antagonistin vitro: The binding of [3H]eltoprazine to whole tissue sections was saturable and revealed an apparent dissociation constant (Kd) of 11 nM. Specific [3H]eltoprazine binding was completely displaced by 5-HT; conversely, unlabelled eltoprazine reduced [3H]5-HT binding to the levels of no...

化合物

p-MPPI hydrochloride

Cat.No: T16421

Target: 5-HT Receptor

Cat.No: T7644

Synonym: Diarylpropionitrile,2,3-双(4-羟苯基)丙腈

Target: Apoptosis, Estrogen Receptor/ERR, Estrogen/progestogen Receptor, Autophagy

Cat.No: T23444

Synonym: N-(4-fluorobenzyl)-2-(1H-indol-3-yl)-2-oxoacetamide

Target: Others

Cat.No: T5828

Synonym: 5-(苄基硫代)-N-甲基-1,3,4-噻二唑-2-胺

Target: GPR

3'-Sialyllactose sodium

Cat.No: T35707

Synonym: 3'-SL sodium

Target: NF-κB

Cat.No: T16401

Target: 5-HT Receptor

Neuropeptide S(Rat)

Cat.No: TP1982

Synonym: Neuropeptide S (Rat)

Neuropeptide S(Rat) TFA

Cat.No: T75951

Neuropeptide S (human)

Cat.No: TP1983

Neuropeptide S(Mouse)

Cat.No: TP1981

Synonym: Neuropeptide S (Mouse)

Neuropeptide S(Mouse) TFA

Cat.No: T75950

α-Helical CRF (9-41) TFA

Cat.No: T83665

Synonym: α-Helical Corticotropin-Releasing Factor (9-41)

SB 242084 dihydrochloride

Cat.No: T37114

Cat.No: T38145

Cat. No.	Product Name	Target	Signaling Pathways
T2940	6-Hydroxyflavone 6-羟基黄酮,6-HF	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	6-Hydroxyflavone (6-HF) 是天然存在的黄酮化合物，具有抗炎作用。它对牛血红蛋白糖基化具有抑制作用。它能激活 AKT、ERK 1/2、JNK 信号通路，有效促进成骨细胞分化。它能抑制 LPS 诱导的 NO 的产生。

天然产物

6-Hydroxyflavone

Cat.No: T2940

Synonym: 6-羟基黄酮,6-HF

Target: GABA Receptor

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼